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This Government Contract opportunity from Department Of Defense was posted on May 7, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Regulatory and Compliance Documentation Services

Closed
Federal

Contract Overview

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The contract involves providing specialized services to prepare and validate essential compliance documentation related to pharmaceutical Requests for Quotations (RFQs). This includes completing Quote Review Checklists, signature pages, and confirming regulatory submissions to ensure adherence to all mandatory compliance standards. The work is aimed at supporting the Defense Health Agency, part of the Department of Defense, emphasizing the importance of stringent regulatory oversight within the healthcare supply chain. Scheduled to be performed in San Antonio, the subcontract opportunity under NAICS code 541611 focuses on management and technical consulting services. The contract's solicitation was posted on May 7, 2026, with a response deadline set for May 28, 2026. The scope underscores the critical need for thorough documentation and validation processes to maintain compliance within pharmaceutical procurement, supporting the Defense Health Agency’s operational and regulatory requirements.

General Info

Provide compliance documentation and validation services for pharmaceutical RFQs supporting Defense Health Agency.

Agency

Department Of Defense → Defense Health Agency (dha)

NAICS

541611 - Administrative Management and General Management Consulting Services View NAICS

Place of Performance

San Antonio, TX, 78230, USA

Set-Aside

NONE

Documents

(0)

No documents available

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Timeline

PhaseClosed
Posted

subcontract

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → Defense Health Agency (dha)
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → Defense Health Agency (dha)
Office AddressN/A
ContactsNo contact information available

Full Description

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Prepare and validate mandatory compliance documentation including Quote Review Checklists, signature pages, and regulatory submission confirmations for pharmaceutical RFQs.